Philips recalls Azurion 3 M15 medical tables with catalog numbers 722064, 722222, and 722280 (OUS only) due to possible patient falls from the table.
Possibility of the patient falling from the table related to the mattress used on the patient table.
Philips is recalling Azurion 3 M15 medical tables because the mattress used on the table might cause patients to fall. This could lead to injuries if the table is not properly secured.
The mattress on the Azurion 3 M15 table may not stay securely attached to the table, increasing the risk of patients falling from the table during medical procedures. This could happen if the mattress is not properly secured or if the table is moved unexpectedly.
Healthcare facilities using Philips Azurion 3 M15 tables with catalog numbers 722064, 722222, or 722280 (for overseas use only) are most at risk. Patients on these tables could fall if the mattress is not securely attached.
Check for catalog numbers 722064, 722222, or 722280 (for overseas use only) on the table. The product is sold under Philips Medical Systems Netherlands B.V.
Look for catalog numbers 722064, 722222, or 722280 (for overseas use only) on the table.
The hazard is that the mattress used on the table might not stay securely attached, increasing the risk of patients falling from the table during medical procedures.
Check for catalog numbers 722064, 722222, or 722280 (for overseas use only) on the table. The product is sold under Philips Medical Systems Netherlands B.V.
The recall record does not specify a remedy, so no action is required beyond checking if your table has the affected catalog numbers.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1154-2025 — Philips Philips Hello, I own a Philips that is covered by recall Z-1154-2025 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
